Variant report

Variant rs150688776
Chromosome Location chr7:50538758-50538759
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:50535800-50539000 Weak transcription Skeletal Muscle Male skeletal muscle
2 chr7:50535800-50540800 Weak transcription Duodenum Mucosa Duodenum
3 chr7:50535800-50546800 Weak transcription Pancreas Pancrea
4 chr7:50535800-50553200 Weak transcription Sigmoid Colon Sigmoid Colon
5 chr7:50536000-50542800 Weak transcription Colonic Mucosa Colon
6 chr7:50536200-50541400 Weak transcription HepG2 liver
7 chr7:50536200-50542200 Strong transcription Fetal Intestine Small intestine
8 chr7:50536200-50545400 Weak transcription Right Atrium heart
9 chr7:50536400-50541400 Weak transcription Colon Smooth Muscle Colon
10 chr7:50536400-50541600 Weak transcription Breast Myoepithelial Primary Cells Breast
11 chr7:50536400-50541800 Strong transcription Fetal Intestine Large intestine
12 chr7:50536600-50543000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
13 chr7:50538200-50538800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr7:50538600-50538800 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
15 chr7:50538600-50538800 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
16 chr7:50538600-50540800 Weak transcription Skeletal Muscle Female skeletal muscle

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